# K212342: ZIIP+ Device

- Pathway: 510(k) (Traditional)
- Applicant: Ziip, Inc.
- Decided: Sep 23, 2021 after 57 days
- Product code: NFO (Stimulator, Transcutaneous Electrical, Aesthetic Purposes)
- Device class: 2
- Regulation: 21 CFR 882.5890
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 5 generations back to K011935 (2001). 7 ancestors in all.
2 later devices descend from it; 2 cite it directly.
0 of 10 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K161484: ZIIP Device, Ziip,Llc (2017) Summary page 4.
- K201782: NuFace Trinity Plus Device, Carol Cole Company Dba Nuface (2021) Summary page 4.

## Most influential descendants
- K232863: Radiant Renewal Skincare Wand (HD-15, HD-15A) (2023), 0 descendants of its own
- K213078: Myolift QT (2023), 0 descendants of its own

## Indications for use
The ZIIP+ Device is indicated for facial and neck stimulation and is indicated for over-the-counter cosmetic use.

Source page: https://510kreport.com/device/K212342
Methodology: https://510kreport.com/methodology